IL1-β was inhibited to its baseline in several, but not all experiments; IL-6 inhibition was always significant but almost never total. As indicated above, IL-10 secretion followed IL-1β and IL-6 secretion. We were surprised to observe that IL-10 was only mildly inhibited relative to IL-1β, and even to IL-6 (Fig. 3C). Inhibition of IL-1β was 75–100% in most experiments, and IL-6 was inhibited 40–70%, whereas IL-10 inhibition was only 20–35%. Thus, interaction with iC3b-opsonized apoptotic cells not only markedly inhibited the proinflammatory response to zymosan, but also changed the relative secretion of cytokines,

favoring a high anti-inflammatory-proinflammatory cytokine secretion ratio. Similar results were obtained while using LPS. IL-1β and IL-6 secretion were reduced from 160±25 to 31±14 and from 1820±188 to 555±88 pg/mL respectively, following one h exposure to opsonized apoptotic cells (p<0.001). In the same manner, https://www.selleckchem.com/products/cetuximab.html interaction with iC3b-opsonized apoptotic cells downregulated MHC class II, CD86, CD83, CD40, and CCR7, as well IL-12 secretion (data not shown, see 5). In order to further RG7422 cell line verify that the decrease in proinflammatory cytokines was not due to decreased ingestion of zymosan, we documented zymosan uptake following

macrophage−apoptotic cell interaction. As shown in Fig. 3D, zymosan uptake was not inhibited following apoptotic cell interaction, and was even augmented. Thus, the inhibitory pattern seen in secretion of proinflammatory cytokines was not due to decreased phagocytosis of zymosan. The specificity of the uptake was further shown by using fibrinogen-coated plates. Zymosan induced proinflammatory cytokines from macrophages differentiated on fibronectin-coated plates,

resulting in IL-1β and IL-6 secretion reaching 197±21 and 2120±118 pg/mL, respectively. Thus, no proinflammatory cytokine inhibition was shown using fibrinogen as a ligand. Furthermore, addition of opsonized apoptotic cells reduced cytokine secretion to 29±11 and 611±48, respectively, following 1 h exposure to opsonized apoptotic cells (p<0.001 and p<0.001). Taken together, the results indicate that CD11b/CD18 and CD11c/CD18 response to ligand is specific to iC3b-opsonized apoptotic cells, and not every ligand (i.e. fibronectin) will induce the same response. Since it has been proposed that inhibition of the proinflammtory response is an autocrine/paracrine process 2, 4, and Methocarbamol we were able to detect IL-10 secretion, we examined the effect of anti-IL-10. As shown in Fig. 4A and B, anti-IL-10 had no effect, suggesting an alternative mode of inhibition. Although TGF-β was not detected, anti-TGF-β was also examined because TGF-β is sometimes hard to detect and can be released in the preformed mode. As shown in Fig. 4A and B, anti-TGF-β did not have any effect on inhibition. Thus, in this system we were not able to demonstrate a paracrine/autocrine effect of IL-10 or TGF-β that led to inhibition of the immune response to zymosan and LPS.